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Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells
MLN4924 is a recently discovered small molecule inhibitor of NEDD8-Activating Enzyme (NAE). Because cullin RING ligase (CRL), the largest family of E3 ubiquitin ligase, requires cullin neddylation for its activity, MLN4924, therefore, acts as an indirect inhibitor of CRL by blocking cullin neddylati...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827092/ https://www.ncbi.nlm.nih.gov/pubmed/27063292 http://dx.doi.org/10.1038/srep24218 |
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author | Lan, Huiyin Tang, Zaiming Jin, Hongchuan Sun, Yi |
author_facet | Lan, Huiyin Tang, Zaiming Jin, Hongchuan Sun, Yi |
author_sort | Lan, Huiyin |
collection | PubMed |
description | MLN4924 is a recently discovered small molecule inhibitor of NEDD8-Activating Enzyme (NAE). Because cullin RING ligase (CRL), the largest family of E3 ubiquitin ligase, requires cullin neddylation for its activity, MLN4924, therefore, acts as an indirect inhibitor of CRL by blocking cullin neddylation. Given that CRLs components are up-regulated, whereas neddylation modification is over-activated in a number of human cancers, MLN4924 was found to be effective in growth suppression of cancer cells. Whether MLN4924 is effective against gastric cancer cells, however, remains elusive. Here we showed that in gastric cancer cells, MLN4924 rapidly inhibited cullin 1 neddylation and remarkably suppressed growth and survival as well as migration in a dose-and time-dependent manner. Mechanistic studies in combination with siRNA knockdown-based rescue experiments revealed that MLN4924 induced the accumulation of a number of CRL substrates, including CDT1/ORC1, p21/p27, and PHLPP1 to trigger DNA damage response and induce growth arrest at the G2/M phase, to induce senescence, as well as autophagy, respectively. MLN4924 also significantly suppressed migration by transcriptionally activating E-cadherin and repressing MMP-9. Taken together, our study suggest that neddylation modification and CRL E3 ligase are attractive gastric cancer targets, and MLN4924 might be further developed as a potent therapeutic agent for the treatment of gastric cancer. |
format | Online Article Text |
id | pubmed-4827092 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-48270922016-04-19 Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells Lan, Huiyin Tang, Zaiming Jin, Hongchuan Sun, Yi Sci Rep Article MLN4924 is a recently discovered small molecule inhibitor of NEDD8-Activating Enzyme (NAE). Because cullin RING ligase (CRL), the largest family of E3 ubiquitin ligase, requires cullin neddylation for its activity, MLN4924, therefore, acts as an indirect inhibitor of CRL by blocking cullin neddylation. Given that CRLs components are up-regulated, whereas neddylation modification is over-activated in a number of human cancers, MLN4924 was found to be effective in growth suppression of cancer cells. Whether MLN4924 is effective against gastric cancer cells, however, remains elusive. Here we showed that in gastric cancer cells, MLN4924 rapidly inhibited cullin 1 neddylation and remarkably suppressed growth and survival as well as migration in a dose-and time-dependent manner. Mechanistic studies in combination with siRNA knockdown-based rescue experiments revealed that MLN4924 induced the accumulation of a number of CRL substrates, including CDT1/ORC1, p21/p27, and PHLPP1 to trigger DNA damage response and induce growth arrest at the G2/M phase, to induce senescence, as well as autophagy, respectively. MLN4924 also significantly suppressed migration by transcriptionally activating E-cadherin and repressing MMP-9. Taken together, our study suggest that neddylation modification and CRL E3 ligase are attractive gastric cancer targets, and MLN4924 might be further developed as a potent therapeutic agent for the treatment of gastric cancer. Nature Publishing Group 2016-04-11 /pmc/articles/PMC4827092/ /pubmed/27063292 http://dx.doi.org/10.1038/srep24218 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lan, Huiyin Tang, Zaiming Jin, Hongchuan Sun, Yi Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells |
title | Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells |
title_full | Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells |
title_fullStr | Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells |
title_full_unstemmed | Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells |
title_short | Neddylation inhibitor MLN4924 suppresses growth and migration of human gastric cancer cells |
title_sort | neddylation inhibitor mln4924 suppresses growth and migration of human gastric cancer cells |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827092/ https://www.ncbi.nlm.nih.gov/pubmed/27063292 http://dx.doi.org/10.1038/srep24218 |
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